A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646281



Internal ID21594586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10344585..10344585hg38UCSC Ensembl
chr11:10366132..10366132hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071988
SamplesHG02818
Known GenesCAND1.11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646281
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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